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Kadsuric acid 3-methylester
Kadsuric acid 3-methylester
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Kadsuric acid 3-methylester
Price:
CAS No.: 1041070-16-9
Catalog No.: CFN92213
Molecular Formula: C31H48O4
Molecular Weight: 484.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The herbs of Kadsura longipedunculata Finet.et Gagnep
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Kadsuric acid 3-methylester is a natural product from Kadsura longipedunculata Finet.et Gagnep.
Kadsuric acid 3-methylester Description
Source: The herbs of Kadsura longipedunculata Finet.et Gagnep
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0631 mL 10.3157 mL 20.6313 mL 41.2626 mL 51.5783 mL
5 mM 0.4126 mL 2.0631 mL 4.1263 mL 8.2525 mL 10.3157 mL
10 mM 0.2063 mL 1.0316 mL 2.0631 mL 4.1263 mL 5.1578 mL
50 mM 0.0413 mL 0.2063 mL 0.4126 mL 0.8253 mL 1.0316 mL
100 mM 0.0206 mL 0.1032 mL 0.2063 mL 0.4126 mL 0.5158 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Helvetica Chimica Acta, 2010 , 91 (5) :856-861.
Terpenoids from Two Dicranopteris Species[Reference: WebLink]

METHODS AND RESULTS:
Two new compounds, (6S,13S)-6-{[β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}cleroda-3,14-dien-13-ol (1) and Kadsuric acid 3-methylester (2), together with nine known compounds, (6S,13E)-6-{[β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}cleroda-3,13-dien-15-ol (3), (6S,13S)-6-[6-O-acetyl-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}-13-{[α-L-rhamnopyranosyl-(1→4)-β-D-fucopyranosyl]oxy}cleroda-3,14-diene (4), (6S,13S)-6-{[6-O-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}-13-{[α-L-rhamnopyranosyl-(1→4)-β-D-fucopyranosyl]oxy}cleroda-3,14-diene (5), 15-hydroxydehydroabietic acid (6), 15-hydroxylabd-8(17)-en-19-oic acid (7), junicedric acid (8), (4β)-kaur-16-en-18-oic acid (9), (4β)-16-hydroxykauran-18-oic acid (10), and (4β,16β)-16-hydroxykauran-18-oic acid (11) were isolated from the fronds of Dicranopteris linearis or D. ampla.
CONCLUSIONS:
Their structures were established by extensive 1D- and 2D-NMR spectroscopy. Compounds 1 and 3–8 showed no anti-HIV activities.
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